A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111237



Internal ID20678277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142519201..142520900hg38UCSC Ensembl
chr4:143440354..143442053hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379909
Supporting Variants
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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